Non-invasive TMS intervention for the abstinence and relapse of addiction

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900024404

Enrollment

Unknown

Registered

2019-07-10

Start date

2019-07-20

Completion date

Unknown

Last updated

2019-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Addiction

Interventions

Group1:10Hz rTMS intervention

Group2:10 Hz sham

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Aged 18-60 years, junior high school degree or above, consent to attend this study.

Exclusion criteria

Exclusion criteria: Have contraindications to TMS (head trauma, epilepsy or the history of epilepsy, metal implant etc.), have contraindication to MRI, psychiatric illnesses, physical ailments, and intellectual impairment (IQ<90).

Design outcomes

Primary

Measure	Time frame
Clinical outcomes;physiological index (Such as blood, feces, etc.);Magnetic Resonance Imaging;Blood Oxygenation Level Dependent;Positron Emission Computed Tomography;Computed Tomography;	—

Secondary

Measure	Time frame
Neuropsychological index (Such as depression, anxiety, craving, sleep, etc.);	—

Countries

China

Contacts

Public ContactWei Lin

The 101st Hospital of PLA

smithlinwx@aliyun.com+86 13812512187

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026